A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25798247



Internal ID19166007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr21:21764717..21916685hg38UCSC Ensembl
Innerchr21:23137037..23289005hg19UCSC Ensembl
Innerchr21:22058908..22210876hg18UCSC Ensembl
Cytoband21q21.1
Allele length
AssemblyAllele length
hg38151969
hg19151969
hg18151969
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893388
Supporting Variants
Samples
Known Genes
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=51
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25798247
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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